Protective effects of resveratrol liposomes on mitochondria in substantia nigra cells of parkinsonized rats

Ann Palliat Med. 2021 Mar;10(3):2458-2468. doi: 10.21037/apm-19-426. Epub 2021 Feb 7.

Abstract

Background: Parkinson's disease (PD) is a central nervous system degenerative disease. The progressive death of dopaminergic neurons is closely correlated to mitochondrial dysfunction. Resveratrol contains three hydroxyl groups, and has a strong neuroprotective effect. This study aimed to investigate the protective effect of resveratrol liposome on mitochondria of substantia nigra cells in Parkinsonized rats through experiment.

Methods: The investigators used 6-hydroxydopamine to establish the Parkinsonized rat model, and used resveratrol liposome from Polygonum cuspidatum (20 mg·kg-1) for gavage, up to a total volume of 1 mL, once-daily, for two weeks. After treatment, the levels of mitochondrial membrane potential, mitochondrial complexes I-IV, mitochondrial cytochrome C, apoptosis-inducing factor (AIF), PTEN-induced putative kinase 1 (PINK1), tumor necrosis factor-receptor-associated protein 1 (TRAP1) and phosphorylated TRAP1 in rat mesencephalic cells were detected according to the operation instructions of the kits.

Results: After two weeks of treatment, resveratrol liposomes could significantly enhance the activity of mitochondrial electron transfer chain complex I in the substantia nigra cells of Parkinsonized model rats, promote the expression of complex I subcomponent MT-ND1-37kD, improve mitochondrial membrane potential, inhibit the release of mitochondrial cytochrome C and apoptotic inducible factor, enhance the expression of mitochondrial functional protein PINK1, increase the phosphorylated TRAP1 level, and elevate the phosphorylated TRAP1/TRAP1 ratio.

Conclusions: Resveratrol liposome has positive effects on mitochondria in substantia nigra cells of Parkinsonized rats, and may be one of its pharmacological mechanisms.

Keywords: Parkinson’s disease; liposomes; mitochondria; rat model; resveratrol.

MeSH terms

  • Animals
  • Disease Models, Animal
  • HSP90 Heat-Shock Proteins / metabolism
  • Liposomes* / metabolism
  • Mitochondria
  • Parkinsonian Disorders*
  • Rats
  • Resveratrol / pharmacology
  • Resveratrol / therapeutic use
  • Substantia Nigra* / metabolism

Substances

  • HSP90 Heat-Shock Proteins
  • Liposomes
  • TRAP1 protein, rat
  • Resveratrol